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Clinical Impact of White Tea and Wheat Grass on Color Enhancement of White Spot Lesions

Not Applicable
Completed
Conditions
White Spot Lesions [Initial Caries] on Smooth Surface of Tooth
Registration Number
NCT06976385
Lead Sponsor
Al-Azhar University
Brief Summary

The current study aimed to evaluate the color change potential of wheat grass and white tea on post orthodontic white spot lesions (WSLs). Materials and Methods: A total of 12 patients were divided into two main groups A1 and A2 according to type of treatment agent (n=6). The A1 group used 10% white tea solution while the A2 group used 10% wheat grass solution. Shade evaluation was conducted using VITA Easyshade V spectrophotometer. Baseline L a b values of WSLs were detected right after orthodontic bracket removal. Patients were requested to rinse with the treatment agent for 1 minute, twice per day. The mean L,a,b values were recorded after 1 month and after 3 months . ΔE values were calculated between baseline, 1 month and 3 months after the treatment agent application and subjected to statistical analysis using one way ANOVA with p\>0.05. Also, Standardized photographs were taken at baseline, after 1 and 3 months. Each WSL was photographed twice with the 1st photograph taken of wet teeth and the 2nd one after prolonged air-drying in order to perform ICDAS II scoring.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
12
Inclusion Criteria
  1. Age range between 15-18 years.
  2. Good oral hygiene
  3. Obvious area of WSL was found around the fixed orthodontic brackets.
  4. Included teeth should be free of any restorations
Exclusion Criteria
  • : 1. Cavitated enamel surface. 2. Presence of any restorations including the labial surface of the involved teeth.
  1. Presence of any environmental or developmental enamel defect such as enamel hypoplasia, fluorosis, stains, and trauma sites on teeth before orthodontic treatment. 4. Allergy to tea and/or wheat

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
ΔE values were calculatedafter 1 month and after 3 months

The mean L,a,b values were recorded . ΔE values were calculated

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Al Azhar University

🇪🇬

Cairo, Egypt

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